Lin LU - NARA Discovery

Novel biallelic LSS variants in autosomal recessive hypotrichosis simplex: insights from a multi-omics approachNARA Subscribed

Human Genetics · 2026 · Vol. 145 · Issue 1 · Springer

Xiaxia Liu; Kai Liu; Yuda Wei; Yongzhen Qi; Yangyang Luo; Tingli Chen; Xiaohua Ye; Junxu Lu; Yunjia Li; Liangqian Jiang; Juan Teng; Xingzhu Geng; Chengcheng Gai; Hongyan Xu; Hui Wang; Lin Li; Chunhai Gao; Xiangyu Zhao

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Exploratory analysis of HLA SNPs associated with occult HBV infection: a multicenter case–control study in Chinese blood donorsNARA Subscribed

Human Genetics · 2026 · Vol. 145 · Issue 1 · Springer

Lin Zhou; Ying Yan; Huimin Ji; Huizhen Sun; Zhuoqun Lu; Le Chang; Lunan Wang

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Decade-long application of preimplantation genetic testing for DMD/BMD: analysis of five clinical strategies and embryo recombination patternsNARA Subscribed

Human Genetics · 2025 · Vol. 144 · Issue 4 · Springer

Weili Wang; Jing Dai; Xiao Hu; Wenbin He; Yifan Gu; Zhenxing Wan; Yi Zhang; Keli Luo; Wen Li; Qianjun Zhang; Fei Gong; Guangxiu Lu; Liang Hu; Yue-Qiu Tan; Ge Lin; Juan Du

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N6-methyladenosine modified lncRNAs signature for stratification of biochemical recurrence in prostate cancerNARA Subscribed

Human Genetics · 2024 · Vol. 143 · Issue 7 · Springer

Yingke Liang; Wenjun Yin; Zhouda Cai; Hongwei Luo; Qinwei Liu; Chuanfan Zhong; Jiahong Chen; Zhuoyuan Lin; Yaqiang Huang; Zhenguo Liang; Junhong Deng; Weide Zhong; Chao Cai; Jianming Lu

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Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes ProjectNARA Subscribed

Human Genetics · 2023 · Vol. 142 · Issue 12 · Springer

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Two novel pleiotropic loci associated with osteoporosis and abdominal obesityNARA Subscribed

Human Genetics · 2020 · Vol. 139 · Issue 8 · Springer

Lu Liu; Xiao-Lin Yang; Hong Zhang; Zi-Jia Zhang; Xin-Tong Wei; Gui-Juan Feng; Ju Liu; Hui-Ping Peng; Rong Hai; Hui Shen; Qing Tian; Hong-Wen Deng; Yu-Fang Pei; Lei Zhang

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Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in ChinaNARA Subscribed

Human Genetics · 2020 · Vol. 139 · Issue 4 · Springer

Huijun Wang; Yulan Lu; Xinran Dong; Guoping Lu; Guoqiang Cheng; Yanyan Qian; Qi Ni; Ping Zhang; Lin Yang; Bingbing Wu; Wenhao Zhou

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Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCDNARA Subscribed

Human Genetics · 2020 · Vol. 139 · Issue 2 · Springer

Chaofeng Tu; Hongchuan Nie; Lanlan Meng; Weili Wang; Haiyu Li; Shimin Yuan; Dehua Cheng; Wenbin He; Gang Liu; Juan Du; Fei Gong; Guangxiu Lu; Ge Lin; Qianjun Zhang; Yue-Qiu Tan

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Genotype imputation for Han Chinese population using Haplotype Reference Consortium as referenceNARA Subscribed

Human Genetics · 2018 · Vol. 137 · Issue 6-7 · Springer

Yuan Lin; Lu Liu; Sen Yang; Yun Li; Dongxin Lin; Xuejun Zhang; Xianyong Yin

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A cis-eQTL genetic variant of the cancer–testis gene CCDC116 is associated with risk of multiple cancersNARA Subscribed

Human Genetics · 2017 · Vol. 136 · Issue 8 · Springer

Na Qin; Cheng Wang; Qun Lu; Tongtong Huang; Meng Zhu; Lihua Wang; Fei Yu; Mingtao Huang; Yue Jiang; Juncheng Dai; Hongxia Ma; Guangfu Jin; Chen Wu; Dongxin Lin; Hongbing Shen; Zhibin Hu

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Integrative multi-omics analysis revealed SNP-lncRNA-mRNA (SLM) networks in human peripheral blood mononuclear cellsNARA Subscribed

Human Genetics · 2017 · Vol. 136 · Issue 4 · Springer

Wei Xia; Xiao-Wei Zhu; Xin-Bo Mo; Long-Fei Wu; Jian Wu; Yu-Fan Guo; Ke-Qin Zeng; Ming-Jun Wang; Xiang Lin; Ying-Hua Qiu; Lan Wang; Pei He; Fang-Fei Xie; Peng-Fei Bing; Xin Lu; Yao-Zhong Liu; Neng-Jun Yi; Fei-Yan Deng; Shu-Feng Lei

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Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA)NARA Subscribed

Human Genetics · 2015 · Vol. 134 · Issue 3 · Springer

H. Dean Hosgood; Minsun Song; Chao Agnes Hsiung; Zhihua Yin; Xiao-Ou Shu; Zhaoming Wang; Nilanjan Chatterjee; Wei Zheng; Neil Caporaso; Laurie Burdette; Meredith Yeager; Sonja I. Berndt; Maria Teresa Landi; Chien-Jen Chen; Gee-Chen Chang; Chin-Fu Hsiao; Ying-Huang Tsai; Li-Hsin Chien; Kuan-Yu Chen; Ming-Shyan Huang; Wu-Chou Su; Yuh-Min Chen; Chung-Hsing Chen; Tsung-Ying Yang; Chih-Liang Wang; Jen-Yu Hung; Chien-Chung Lin; Reury-Perng Perng; Chih-Yi Chen; Kun-Chieh Chen; Yao-Jen Li; Chong-Jen Yu; Yi-Song Chen; Ying-Hsiang Chen; Fang-Yu Tsai; Christopher Kim; Wei Jie Seow; Bryan A. Bassig; Wei Wu; Peng Guan; Qincheng He; Yu-Tang Gao; Qiuyin Cai; Wong-Ho Chow; Yong-Bing Xiang; Dongxin Lin; Chen Wu; Yi-Long Wu; Min-Ho Shin; Yun-Chul Hong; Keitaro Matsuo; Kexin Chen; Maria Pik Wong; Dara Lu; Li Jin; Jiu-Cun Wang; Adeline Seow; Tangchun Wu; Hongbing Shen; Joseph F. Fraumeni; Pan-Chyr Yang; I-Shou Chang; Baosen Zhou; Stephen J. Chanock; Nathaniel Rothman; Qing Lan

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Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial diseaseNARA Subscribed

Human Genetics · 2014 · Vol. 133 · Issue 3 · Springer

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HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)NARA Subscribed

Human Genetics · 2013 · Vol. 132 · Issue 1 · Springer

Jianfeng Xu; Ethan M. Lange; Lingyi Lu; Siqun L. Zheng; Zhong Wang; Stephen N. Thibodeau; Lisa A. Cannon-Albright; Craig C. Teerlink; Nicola J. Camp; Anna M. Johnson; Kimberly A. Zuhlke; Janet L. Stanford; Elaine A. Ostrander; Kathleen E. Wiley; Sarah D. Isaacs; Patrick C. Walsh; Christiane Maier; Manuel Luedeke; Walther Vogel; Johanna Schleutker; Tiina Wahlfors; Teuvo Tammela; Daniel Schaid; Shannon K. McDonnell; Melissa S. DeRycke; Geraldine Cancel-Tassin; Olivier Cussenot; Fredrik Wiklund; Henrik Grönberg; Ros Eeles; Doug Easton; Zsofia Kote-Jarai; Alice S. Whittemore; Chih-Lin Hsieh; Graham G. Giles; John L. Hopper; Gianluca Severi; William J. Catalona; Diptasri Mandal; Elisa Ledet; William D. Foulkes; Nancy Hamel; Lovise Mahle; Pal Moller; Isaac Powell; Joan E. Bailey-Wilson; John D. Carpten; Daniela Seminara; Kathleen A. Cooney; William B. Isaacs

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Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in AsiaNARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 7 · Springer

H. Dean Hosgood; Wen-Chang Wang; Yun-Chul Hong; Jiu-Cun Wang; Kexin Chen; I-Shou Chang; Chien-Jen Chen; Daru Lu; Zhihua Yin; Chen Wu; Wei Zheng; Biyun Qian; Jae Yong Park; Yeul Hong Kim; Nilanjan Chatterjee; Ying Chen; Gee-Chen Chang; Chin-Fu Hsiao; Meredith Yeager; Ying-Huang Tsai; Hu Wei; Young Tae Kim; Wei Wu; Zhenhong Zhao; Wong-Ho Chow; Xiaoling Zhu; Yen-Li Lo; Sook Whan Sung; Kuan-Yu Chen; Jeff Yuenger; Joo Hyun Kim; Liming Huang; Ying-Hsiang Chen; Yu-Tang Gao; Jin Hee Kim; Ming-Shyan Huang; Tae Hoon Jung; Neil Caporaso; Xueying Zhao; Zhang Huan; Dianke Yu; Chang Ho Kim; Wu-Chou Su; Xiao-Ou Shu; In-San Kim; Bryan Bassig; Yuh-Min Chen; Sung Ick Cha; Wen Tan; Hongyan Chen; Tsung-Ying Yang; Jae Sook Sung; Chih-Liang Wang; Xuelian Li; Kyong Hwa Park; Chong-Jen Yu; Jeong-Seon Ryu; Yongbing Xiang; Amy Hutchinson; Jun Suk Kim; Qiuyin Cai; Maria Teresa Landi; Kyoung-Mu Lee; Jen-Yu Hung; Ju-Yeon Park; Margaret Tucker; Chien-Chung Lin; Yangwu Ren; Reury-Perng Perng; Chih-Yi Chen; Li Jin; Kun-Chieh Chen; Yao-Jen Li; Yu-Fang Chiu; Fang-Yu Tsai; Pan-Chyr Yang; Joseph F. Fraumeni; Adeline Seow; Dongxin Lin; Baosen Zhou; Stephen Chanock; Chao Agnes Hsiung; Nathaniel Rothman; Qing Lan

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Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)NARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 7 · Springer

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Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese HansNARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer

Ling Lu; Hongguang Sheng; Huaixing Li; Wei Gan; Chen Liu; Jingwen Zhu; Ruth J. F. Loos; Xu Lin

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Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IINARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer

Hua Zhang; Hongsheng Chen; Hunjin Luo; Jing An; Lin Sun; Lingyun Mei; Chufeng He; Lu Jiang; Wen Jiang; Kun Xia; Jia-Da Li; Yong Feng

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A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitisNARA Subscribed

Human Genetics · 2003 · Vol. 113 · Issue 5 · Springer

Min Wang; Zhi-Min Xing; Chao Lu; You-Xiang Ma; De-Lin Yu; Zheng Yan; Shen-Wu Wang; Li-Sheng Yu

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